A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927298



Internal ID18911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173836154..173836549hg38UCSC Ensembl
chr2:174700882..174701277hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437412
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927298
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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